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Evidence Generation Intern

0-2 years
Not Disclosed
10 Dec. 18, 2025
Job Description
Job Type: Full Time Hybrid Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Evidence Generation Intern | Princeton, NJ

Job ID: R14894
Category: Research & Discovery
Location: Princeton, New Jersey, United States
Job Type: Internship (June – August 2026, Hybrid)


About Genmab

Genmab is a global biotechnology leader focused on improving patient outcomes through innovative antibody therapeutics. With 25+ years of experience, the company has developed next-generation platforms, including bispecific T-cell engagers, antibody-drug conjugates, immune checkpoint modulators, and effector function-enhanced antibodies.

Headquartered in Copenhagen, Denmark, Genmab operates across North America, Europe, and Asia-Pacific, aiming to transform cancer and serious disease treatment with Knock-Your-Socks-Off (KYSO®) antibody medicines.

Learn more at www.genmab.com.


Internship Overview

The Evidence Generation Intern will gain practical experience supporting Investigator-Driven Programs and Managed Access Programs within Genmab’s Medical Affairs team. This internship provides exposure to operational aspects of Investigator-Sponsored Trials (ISTs), Collaborative Research Trials (CRTs), and other evidence generation initiatives, building a foundation for careers in clinical research and medical affairs.

The internship follows a hybrid schedule, with 3 days onsite in Princeton, NJ, and 2 days remote per week.


Key Responsibilities

  • Assist in the implementation of Investigator-Driven and Managed Access Programs.

  • Support governance meetings to ensure successful program execution.

  • Track operational timelines and deliverables across programs.

  • Manage study and program proposals from submission through study closure.

  • Support budget and timeline adherence for investigator-driven programs.

  • Collaborate with cross-functional teams to adjust project milestones as needed.

  • Generate metrics and reports for program activities.

  • Participate in mentorship sessions and contribute to discussions on process improvement and best practices.


Required Qualifications

  • Currently enrolled in a Bachelor’s or Advanced degree in a scientific discipline.

  • Strong analytical and problem-solving skills.

  • Excellent written and verbal communication skills.

  • Ability to work both independently and as part of a collaborative team.

  • Attention to detail and quality while managing multiple tasks.


Preferred Qualifications

  • Basic understanding of clinical research.

  • Demonstrates initiative, proactivity, and eagerness to learn in a fast-paced environment.

  • Effective communication and collaboration with mentors, stakeholders, and team members.


Internship Benefits

  • Hands-on experience in clinical research operations and evidence generation.

  • Exposure to investigator-driven programs and managed access initiatives.

  • Mentorship and networking opportunities within Medical Affairs and cross-functional teams.

  • Professional development through process improvement and operational excellence projects.


About You

  • Passionate about clinical research, medical affairs, and innovation.

  • Collaborative and adaptable in a dynamic, fast-growing environment.

  • Proactive, detail-oriented, and solution-focused.

  • Committed to excellence and continuous learning.